A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659418



Internal ID15396070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34647083..34650770hg38UCSC Ensembl
Innerchr14:35116289..35119976hg19UCSC Ensembl
Innerchr14:34186040..34189727hg18UCSC Ensembl
Innerchr14:34186040..34189727hg17UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg383688
hg193688
hg183688
hg173688
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516595
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659418
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer